LON蛋白酶1在疾病中的研究进展
DOI:
作者:
作者单位:

南京医科大学附属儿童医院

作者简介:

通讯作者:

中图分类号:

基金项目:


Advances of Lon protease 1 in diseases
Author:
Affiliation:

1.children'2.'3.s hospital of Nanjing medical university

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    线粒体是人体的能量代谢中心,不仅通过氧化磷酸化为生命活动提供能量,还参与调控物质代谢、细胞凋亡、信号转导、活性氧平衡等过程,线粒体稳态平衡在维持细胞微环境稳定与器官正常功能中至关重要。LON蛋白酶1(LON protease 1,LONP1)是一种核基因LONP1(PRSS15)编码的、在进化中高度保守的、发挥多种生物学功能的三磷酸腺苷(Adenosine triphosphate,ATP)依赖性的丝氨酸蛋白酶。它主要定位于线粒体基质,具有清除错误折叠和氧化修饰的蛋白质、稳定线粒体DNA(Mitochondrial DNA,mtDNA)和扮演分子伴侣的功能,是维持线粒体稳态平衡、蛋白质量控制的关键蛋白酶。近年来,LONP1通过调控线粒体质量和能量控制系统,参与个体发育、器官衰老和各类疾病的发生发展的研究日益增多。文章系统综述了LONP1的生物学特征、结构及功能,及其在胚胎发育和衰老、癌症和各类疾病中的研究进展。

    Abstract:

    Mitochondria serve as the central hub of cellular energy metabolism. Beyond generating ATP via oxidative phosphorylation to sustain vital activities, they participate in regulating material metabolism, apoptosis, signal transduction, and reactive oxygen species homeostasis. Maintenance of mitochondrial homeostasis is indispensable for preserving intracellular microenvironmental stability and the physiological function of organs. LON protease 1 (LONP1) is an ATP-dependent protease encoded by the nuclear gene LONP1 (PRSS15), which is highly conserved and involved in various biological functions. LONP1, located in the mitochondrial matrix, plays a key role in maintaining mitochondrial homeostasis and protein quality control and participates in removing misfolded and oxidative modified protein, binding mitochondrial DNA (mtDNA), and being a molecular chaperone. To date, there is growing evidence that LONP1, through its regulation of mitochondrial quality and energy homeostasis, is involved in development, aging, and various diseases. This article will review the biological characteristics, structure, and function of LONP1, as well as the advances of LONP1 in embryonic development, aging, cancer, and various diseases.

    参考文献
    相似文献
    引证文献
引用本文
分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:2025-08-18
  • 最后修改日期:2025-11-13
  • 录用日期:2025-12-26
  • 在线发布日期:
  • 出版日期:
关闭